| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:96333622-96333801 | Rare:39 | ||||
| chr15:99251188-99251516 | Common:4; Rare:119 | ||||
| chr15:100602167-100602640 | Common:3; Rare:126 | ||||
| chr15:101295174-101295354 | Rare:55 | ||||
| chr15:101652276-101652529 | Common:5; Rare:125 | ||||
| chr16:53590-53908 | Common:7; Rare:109 | ||||
| chr16:72525-72744 | Common:10; Rare:58 | ||||
| chr16:77912-78312 | Common:5; Rare:132 | ||||
| chr16:138661-138764 | Common:2; Rare:28 | ||||
| chr16:229113-229236 | Common:2; Rare:52 | ||||
| chr16:401738-401962 | Common:1; Rare:96 | ||||
| chr16:684326-684464 | Common:2; Rare:72 | ||||
| chr16:1351778-1351980 | Common:2; Rare:96; Clinvar:6; Clinvar (benign):1 | ||||
| chr16:1420714-1420902 | Common:1; Rare:77 | ||||
| chr16:1533474-1533694 | Common:2; Rare:41 |